Senior Nonclinical Writer and Study Coordinator @ (October 2019 - January 2022)
Nonclinical Regulatory Submission Lead Writer @ (January 2018 - October 2019)
Manager, Early Development Nonclinical Technical Writing @ (August 2016 - January 2018)
Associate Project Manager, Early Phase Development Solutions @ (December 2014 - August 2016)
Nonclinical Writing Associate, Global Medical and Regulatory Writing @ (December 2011 - December 2014)
Study Coordinator, Bioanalytical Chemistry @ (July 2010 - December 2011)
Study Technician and Research Assistant, Anatomic Pathology @ (October 2008 - July 2010)
Study Technician, Dose Formulations @ (July 2006 - November 2008)
Lisa Johnsen Education
Northern Michigan University
Bachelor of Science (BS) (Biology/Ecology Emphasis)
2002-2006
Lisa Johnsen Skills
GLP
CRO
Toxicology
Chemistry
Drug Development
GCP
In Vivo
Drug Discovery
Pharmaceutical Industry
Biotechnology
Pharmacology
Clinical Development
Clinical Trials
Validation
Lifesciences
FDA
LIMS
HPLC
Analytical Chemistry
Protocol
In Vitro
GMP
Regulatory Affairs
Life Sciences
Project management
CPM
CRO Management
Good Laboratory Practice (GLP)
U.S. Food and Drug Administration (FDA)
Social Media
Good Laboratory Practice Glp
Blogging
Troubleshooting
Microsoft Office
SQL
Research
Good Laboratory Practice
Lisa Johnsen Summary
Lisa Johnsen, based in United States, is currently a Associate Director, Medical Writing at Hemab Therapeutics. Lisa Johnsen brings experience from previous roles at Novo Nordisk, Cardinal Health, Dicerna Pharmaceuticals, Inc. and Takeda. Lisa Johnsen holds a 2002 - 2006 Bachelor of Science (BS) in Biology/Ecology Emphasis @ Northern Michigan University. With a robust skill set that includes GLP, CRO, Toxicology, Chemistry, Drug Development and more. Lisa Johnsen has 2 emails and 2 mobile phone numbers on RocketReach.
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